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Artigo de periodico
Como é realizada a indicação de medicamentos por farmacêuticos comunitários no Brasil? (2022)
Mota, Karolini De Faria; Oliveira, William Neves ; Pereira, Mariana Linhares ; Baptista, Elaine Cristina Coelho; Reis, Tiago Marques dos; Pereira, Leonardo Régis Leira ; Nascimento, Mariana Martins Gonzaga do ; Obreli Neto, Paulo Roque ; Aguiar, Patrícia Melo ; Baldoni, André Oliveira
Source: Revista Brasileira de Pesquisa em Saúde. Unidades: FCFRP, FCF
Subjects: MEDICAMENTO, PRÁTICA CLÍNICA
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ABNT
MOTA, Karolini De Faria et al. Como é realizada a indicação de medicamentos por farmacêuticos comunitários no Brasil?. Revista Brasileira de Pesquisa em Saúde, v. 23, n. 2 p. 49-54, 2022Tradução . . Disponível em: https://doi.org/10.47456/rbps.v23i2.34126. Acesso em: 15 nov. 2024.
APA
Mota, K. D. F., Oliveira, W. N., Pereira, M. L., Baptista, E. C. C., Reis, T. M. dos, Pereira, L. R. L., et al. (2022). Como é realizada a indicação de medicamentos por farmacêuticos comunitários no Brasil? Revista Brasileira de Pesquisa em Saúde, 23( 2 p. 49-54). doi:10.47456/rbps.v23i2.34126
NLM
Mota KDF, Oliveira WN, Pereira ML, Baptista ECC, Reis TM dos, Pereira LRL, Nascimento MMG do, Obreli Neto PR, Aguiar PM, Baldoni AO. Como é realizada a indicação de medicamentos por farmacêuticos comunitários no Brasil? [Internet]. Revista Brasileira de Pesquisa em Saúde. 2022 ; 23( 2 p. 49-54):[citado 2024 nov. 15 ] Available from: https://doi.org/10.47456/rbps.v23i2.34126
Vancouver
Mota KDF, Oliveira WN, Pereira ML, Baptista ECC, Reis TM dos, Pereira LRL, Nascimento MMG do, Obreli Neto PR, Aguiar PM, Baldoni AO. Como é realizada a indicação de medicamentos por farmacêuticos comunitários no Brasil? [Internet]. Revista Brasileira de Pesquisa em Saúde. 2022 ; 23( 2 p. 49-54):[citado 2024 nov. 15 ] Available from: https://doi.org/10.47456/rbps.v23i2.34126
Artigo de periodico
Gold-coated superparamagnetic iron oxide nanoparticles attenuate collagen-induced arthritis after magnetic targeting (2020)
Carneiro, Maria Fernanda Hornos ; Machado, Ana Rita Thomazela ; Antunes, Lusânia Maria Greggi ; Souza, Talita E.; Freitas, Victor A.; Oliveira, Luiz C. A.; Rodrigues, Jairo L.; Pereira, Marcio C.; Barbosa Junior, Fernando
Source: Biological Trace Element Research. Unidade: FCFRP
Subjects: NANOPARTÍCULAS, OURO, INFLAMAÇÃO, MAGNETISMO, ARTRITE, COLÁGENO
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ABNT
CARNEIRO, Maria Fernanda Hornos et al. Gold-coated superparamagnetic iron oxide nanoparticles attenuate collagen-induced arthritis after magnetic targeting. Biological Trace Element Research, v. 194, n. 2, p. 502-513, 2020Tradução . . Disponível em: https://doi.org/10.1007/s12011-019-01799-z. Acesso em: 15 nov. 2024.
APA
Carneiro, M. F. H., Machado, A. R. T., Antunes, L. M. G., Souza, T. E., Freitas, V. A., Oliveira, L. C. A., et al. (2020). Gold-coated superparamagnetic iron oxide nanoparticles attenuate collagen-induced arthritis after magnetic targeting. Biological Trace Element Research, 194( 2), 502-513. doi:10.1007/s12011-019-01799-z
NLM
Carneiro MFH, Machado ART, Antunes LMG, Souza TE, Freitas VA, Oliveira LCA, Rodrigues JL, Pereira MC, Barbosa Junior F. Gold-coated superparamagnetic iron oxide nanoparticles attenuate collagen-induced arthritis after magnetic targeting [Internet]. Biological Trace Element Research. 2020 ; 194( 2): 502-513.[citado 2024 nov. 15 ] Available from: https://doi.org/10.1007/s12011-019-01799-z
Vancouver
Carneiro MFH, Machado ART, Antunes LMG, Souza TE, Freitas VA, Oliveira LCA, Rodrigues JL, Pereira MC, Barbosa Junior F. Gold-coated superparamagnetic iron oxide nanoparticles attenuate collagen-induced arthritis after magnetic targeting [Internet]. Biological Trace Element Research. 2020 ; 194( 2): 502-513.[citado 2024 nov. 15 ] Available from: https://doi.org/10.1007/s12011-019-01799-z
Trabalho de evento-resumo
Synthesis and docking study for compounds analogs of LSD1 inhibitor (2019)
Lima, Elys Juliane Cardoso; Maltarollo, Vinícius Gonçalves ; Ganesan, Arasu; Emery, Flavio da Silva ; Wünsch, B; Trossini, Gustavo Henrique Goulart
Source: Abstracts. Conference titles: Brazilian Symposium on Medicinal Chemistry - BrazMedChem. Unidades: FCFRP, FCF
Subjects: NEOPLASIAS, COMPOSTOS HETEROCÍCLICOS
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ABNT
LIMA, Elys Juliane Cardoso et al. Synthesis and docking study for compounds analogs of LSD1 inhibitor. 2019, Anais.. Campinas: Galoá, 2019. Disponível em: https://proceedings.science/brazmed-chem-2019/trabajos. Acesso em: 15 nov. 2024.
APA
Lima, E. J. C., Maltarollo, V. G., Ganesan, A., Emery, F. da S., Wünsch, B., & Trossini, G. H. G. (2019). Synthesis and docking study for compounds analogs of LSD1 inhibitor. In Abstracts. Campinas: Galoá. Recuperado de https://proceedings.science/brazmed-chem-2019/trabajos
NLM
Lima EJC, Maltarollo VG, Ganesan A, Emery F da S, Wünsch B, Trossini GHG. Synthesis and docking study for compounds analogs of LSD1 inhibitor [Internet]. Abstracts. 2019 ;[citado 2024 nov. 15 ] Available from: https://proceedings.science/brazmed-chem-2019/trabajos
Vancouver
Lima EJC, Maltarollo VG, Ganesan A, Emery F da S, Wünsch B, Trossini GHG. Synthesis and docking study for compounds analogs of LSD1 inhibitor [Internet]. Abstracts. 2019 ;[citado 2024 nov. 15 ] Available from: https://proceedings.science/brazmed-chem-2019/trabajos
Artigo de periodico
Association between heavy metal exposure and poor working memory and possible mediation effect of antioxidant defenses during aging (2017)
Talarico, Juliana Nery de Souza; Marcourakis, Tania ; Barbosa Júnior, Fernando; Barros, Silvia Berlanga de Moraes ; Rivelli, Diogo Pineda; Pompéia, Sabine; Caramelli, Paulo; Plusquellec, Pierrich; Lupien, Sonia J; Catucci, Raphael Fernandes; Alves, Andréa Regiani; Suchecki, Deborah
Source: Science of the Total Environmental. Unidades: EE, FCF, FCFRP
Subjects: METAIS PESADOS, ANTIOXIDANTES
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ABNT
TALARICO, Juliana Nery de Souza et al. Association between heavy metal exposure and poor working memory and possible mediation effect of antioxidant defenses during aging. Science of the Total Environmental, v. 575, p. 750-757, 2017Tradução . . Disponível em: https://doi.org/10.1016/j.scitotenv.2016.09.121. Acesso em: 15 nov. 2024.
APA
Talarico, J. N. de S., Marcourakis, T., Barbosa Júnior, F., Barros, S. B. de M., Rivelli, D. P., Pompéia, S., et al. (2017). Association between heavy metal exposure and poor working memory and possible mediation effect of antioxidant defenses during aging. Science of the Total Environmental, 575, 750-757. doi:10.1016/j.scitotenv.2016.09.121
NLM
Talarico JN de S, Marcourakis T, Barbosa Júnior F, Barros SB de M, Rivelli DP, Pompéia S, Caramelli P, Plusquellec P, Lupien SJ, Catucci RF, Alves AR, Suchecki D. Association between heavy metal exposure and poor working memory and possible mediation effect of antioxidant defenses during aging [Internet]. Science of the Total Environmental. 2017 ; 575 750-757.[citado 2024 nov. 15 ] Available from: https://doi.org/10.1016/j.scitotenv.2016.09.121
Vancouver
Talarico JN de S, Marcourakis T, Barbosa Júnior F, Barros SB de M, Rivelli DP, Pompéia S, Caramelli P, Plusquellec P, Lupien SJ, Catucci RF, Alves AR, Suchecki D. Association between heavy metal exposure and poor working memory and possible mediation effect of antioxidant defenses during aging [Internet]. Science of the Total Environmental. 2017 ; 575 750-757.[citado 2024 nov. 15 ] Available from: https://doi.org/10.1016/j.scitotenv.2016.09.121
Artigo de periodico
Factors that motivate healthcare professionals to report adverse drug events: a systematic review (2017)
Abjaude, Samir Antonio Rodrigues; Mieli, Stephania Furlaneto; Magalhães, Zídia Rocha; Pereira, Leonardo Régis Leira
Source: Pharmaceutical Medicine. Unidade: FCFRP
Subjects: MEDICAMENTO, REVISÃO SISTEMÁTICA
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ABNT
ABJAUDE, Samir Antonio Rodrigues et al. Factors that motivate healthcare professionals to report adverse drug events: a systematic review. Pharmaceutical Medicine, v. 31, n. 1, p. 13-20, 2017Tradução . . Disponível em: https://link.springer.com/article/10.1007/s40290-016-0174-2. Acesso em: 15 nov. 2024.
APA
Abjaude, S. A. R., Mieli, S. F., Magalhães, Z. R., & Pereira, L. R. L. (2017). Factors that motivate healthcare professionals to report adverse drug events: a systematic review. Pharmaceutical Medicine, 31( 1), 13-20. Recuperado de https://link.springer.com/article/10.1007/s40290-016-0174-2
NLM
Abjaude SAR, Mieli SF, Magalhães ZR, Pereira LRL. Factors that motivate healthcare professionals to report adverse drug events: a systematic review [Internet]. Pharmaceutical Medicine. 2017 ; 31( 1): 13-20.[citado 2024 nov. 15 ] Available from: https://link.springer.com/article/10.1007/s40290-016-0174-2
Vancouver
Abjaude SAR, Mieli SF, Magalhães ZR, Pereira LRL. Factors that motivate healthcare professionals to report adverse drug events: a systematic review [Internet]. Pharmaceutical Medicine. 2017 ; 31( 1): 13-20.[citado 2024 nov. 15 ] Available from: https://link.springer.com/article/10.1007/s40290-016-0174-2
Trabalho de evento-resumo
Virtual screening applied in hit identification as LSD1 inhibitors, a epigenetic target for cancer treatment (2017)
Lima, Elys Juliane Cardoso; Maltarollo, Vinícius Gonçalves; Ganesan, Arasu; Emery, Flavio da Silva; Trossini, Gustavo Henrique Goulart
Source: Proceedings. Conference titles: World Chemistry Congress. Unidades: FCFRP, FCF
Subjects: INIBIDORES DE ENZIMAS, ANTINEOPLÁSICOS
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ABNT
LIMA, Elys Juliane Cardoso et al. Virtual screening applied in hit identification as LSD1 inhibitors, a epigenetic target for cancer treatment. 2017, Anais.. Durham: International Union of Pure and Applied Chemistry (IUPAC), 2017. Disponível em: http://www.neopixdmi.com.br/@mci/iupac2017/. Acesso em: 15 nov. 2024.
APA
Lima, E. J. C., Maltarollo, V. G., Ganesan, A., Emery, F. da S., & Trossini, G. H. G. (2017). Virtual screening applied in hit identification as LSD1 inhibitors, a epigenetic target for cancer treatment. In Proceedings. Durham: International Union of Pure and Applied Chemistry (IUPAC). Recuperado de http://www.neopixdmi.com.br/@mci/iupac2017/
NLM
Lima EJC, Maltarollo VG, Ganesan A, Emery F da S, Trossini GHG. Virtual screening applied in hit identification as LSD1 inhibitors, a epigenetic target for cancer treatment [Internet]. Proceedings. 2017 ;[citado 2024 nov. 15 ] Available from: http://www.neopixdmi.com.br/@mci/iupac2017/
Vancouver
Lima EJC, Maltarollo VG, Ganesan A, Emery F da S, Trossini GHG. Virtual screening applied in hit identification as LSD1 inhibitors, a epigenetic target for cancer treatment [Internet]. Proceedings. 2017 ;[citado 2024 nov. 15 ] Available from: http://www.neopixdmi.com.br/@mci/iupac2017/
Artigo de periodico
Direct visualization of neurotransmitters in rat brain slices by desorption electrospray ionization mass spectrometry imaging (DESI - MS) (2016)
Fernandes, Anna Maria A. P.; Vendramini, Pedro H.; Galaverna, Renan; Schwab, Nicolas V.; Alberici, Luciane Carla; Augusti, Rodinei; Castilho, Roger F.; Eberlin, Marcos N.
Source: Journal of The American Society for Mass Spectrometry. Unidade: FCFRP
Subjects: ESPECTROMETRIA DE MASSAS, NEUROTRANSMISSORES, CÉREBRO
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ABNT
FERNANDES, Anna Maria A. P. et al. Direct visualization of neurotransmitters in rat brain slices by desorption electrospray ionization mass spectrometry imaging (DESI - MS). Journal of The American Society for Mass Spectrometry, v. 27, n. 12, p. 1944-1951, 2016Tradução . . Disponível em: https://doi.org/10.1007/s13361-016-1475-0. Acesso em: 15 nov. 2024.
APA
Fernandes, A. M. A. P., Vendramini, P. H., Galaverna, R., Schwab, N. V., Alberici, L. C., Augusti, R., et al. (2016). Direct visualization of neurotransmitters in rat brain slices by desorption electrospray ionization mass spectrometry imaging (DESI - MS). Journal of The American Society for Mass Spectrometry, 27( 12), 1944-1951. doi:10.1007/s13361-016-1475-0
NLM
Fernandes AMAP, Vendramini PH, Galaverna R, Schwab NV, Alberici LC, Augusti R, Castilho RF, Eberlin MN. Direct visualization of neurotransmitters in rat brain slices by desorption electrospray ionization mass spectrometry imaging (DESI - MS) [Internet]. Journal of The American Society for Mass Spectrometry. 2016 ; 27( 12): 1944-1951.[citado 2024 nov. 15 ] Available from: https://doi.org/10.1007/s13361-016-1475-0
Vancouver
Fernandes AMAP, Vendramini PH, Galaverna R, Schwab NV, Alberici LC, Augusti R, Castilho RF, Eberlin MN. Direct visualization of neurotransmitters in rat brain slices by desorption electrospray ionization mass spectrometry imaging (DESI - MS) [Internet]. Journal of The American Society for Mass Spectrometry. 2016 ; 27( 12): 1944-1951.[citado 2024 nov. 15 ] Available from: https://doi.org/10.1007/s13361-016-1475-0
Artigo de periodico
Structural and functional elucidation of peptide Ts11 shows evidence of a novel subfamily of scorpion venom toxins (2016)
Cremonez, Caroline M.; Maiti, Mohitosh; Peigneur, Steve; Cassoli, Juliana Silva ; Dutra, Alexandre A. A.; Waekens, Etienne; Lescrinier, Eveline; Herdewijn, Piet; Lima, Maria Elena de; Pimenta, Adriano M. C.; Arantes, Eliane Candiani; Tytgat, Jan
Source: Toxins. Unidade: FCFRP
Subjects: TOXINAS, VENENOS DE ORIGEM ANIMAL, ESCORPIÕES, ELETROFISIOLOGIA, PEPTÍDEOS
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ABNT
CREMONEZ, Caroline M. et al. Structural and functional elucidation of peptide Ts11 shows evidence of a novel subfamily of scorpion venom toxins. Toxins, v. 8, 2016Tradução . . Disponível em: https://doi.org/10.3390/toxins8100288. Acesso em: 15 nov. 2024.
APA
Cremonez, C. M., Maiti, M., Peigneur, S., Cassoli, J. S., Dutra, A. A. A., Waekens, E., et al. (2016). Structural and functional elucidation of peptide Ts11 shows evidence of a novel subfamily of scorpion venom toxins. Toxins, 8. doi:10.3390/toxins8100288
NLM
Cremonez CM, Maiti M, Peigneur S, Cassoli JS, Dutra AAA, Waekens E, Lescrinier E, Herdewijn P, Lima ME de, Pimenta AMC, Arantes EC, Tytgat J. Structural and functional elucidation of peptide Ts11 shows evidence of a novel subfamily of scorpion venom toxins [Internet]. Toxins. 2016 ; 8[citado 2024 nov. 15 ] Available from: https://doi.org/10.3390/toxins8100288
Vancouver
Cremonez CM, Maiti M, Peigneur S, Cassoli JS, Dutra AAA, Waekens E, Lescrinier E, Herdewijn P, Lima ME de, Pimenta AMC, Arantes EC, Tytgat J. Structural and functional elucidation of peptide Ts11 shows evidence of a novel subfamily of scorpion venom toxins [Internet]. Toxins. 2016 ; 8[citado 2024 nov. 15 ] Available from: https://doi.org/10.3390/toxins8100288
Artigo de periodico
Protective effects of the angiotensin type 1 receptor antagonist losartan in infection-induced and arthritis-associated alveolar bone loss (2015)
Queiroz-Júnior, Celso Martins; Silveira, K. D.; Oliveira, C. R. de; Moura, A. P.; Madeira, M. F. M.; Soriani, Frederico Marianetti; Ferreira, A. J.; Fukada, Sandra Yasuyo; Teixeira, M. M.; Souza, D. G.; Silva, T. A. da
Source: Journal of Periodontal Research. Unidade: FCFRP
Subjects: ARTRITE, ANGIOTENSINAS, DOENÇAS ÓSSEAS, ANTI-INFLAMATÓRIOS, OSTEOBLASTO
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ABNT
QUEIROZ-JÚNIOR, Celso Martins et al. Protective effects of the angiotensin type 1 receptor antagonist losartan in infection-induced and arthritis-associated alveolar bone loss. Journal of Periodontal Research, v. 50, n. 6, p. 814–823, 2015Tradução . . Disponível em: https://doi.org/10.1111/jre.12269. Acesso em: 15 nov. 2024.
APA
Queiroz-Júnior, C. M., Silveira, K. D., Oliveira, C. R. de, Moura, A. P., Madeira, M. F. M., Soriani, F. M., et al. (2015). Protective effects of the angiotensin type 1 receptor antagonist losartan in infection-induced and arthritis-associated alveolar bone loss. Journal of Periodontal Research, 50( 6), 814–823. doi:10.1111/jre.12269
NLM
Queiroz-Júnior CM, Silveira KD, Oliveira CR de, Moura AP, Madeira MFM, Soriani FM, Ferreira AJ, Fukada SY, Teixeira MM, Souza DG, Silva TA da. Protective effects of the angiotensin type 1 receptor antagonist losartan in infection-induced and arthritis-associated alveolar bone loss [Internet]. Journal of Periodontal Research. 2015 ; 50( 6): 814–823.[citado 2024 nov. 15 ] Available from: https://doi.org/10.1111/jre.12269
Vancouver
Queiroz-Júnior CM, Silveira KD, Oliveira CR de, Moura AP, Madeira MFM, Soriani FM, Ferreira AJ, Fukada SY, Teixeira MM, Souza DG, Silva TA da. Protective effects of the angiotensin type 1 receptor antagonist losartan in infection-induced and arthritis-associated alveolar bone loss [Internet]. Journal of Periodontal Research. 2015 ; 50( 6): 814–823.[citado 2024 nov. 15 ] Available from: https://doi.org/10.1111/jre.12269
Artigo de periodico
Enhancement on reactive oxygen species and COX-1 mRNA levels modulate the vascular relaxation induced by sodium nitroprusside in denuded mice aorta (2015)
Kangussu, Lucas M.; Olivon, Vania C.; Arifa, Raquel D. do N.; Araújo, Natália; Reis, Daniela; Assis, Marieta T. de A.; Soriani, Frederico M.; Souza, Daniele da G. de; Bendhack, Lusiane Maria; Bonaventura, Daniella
Source: Fundamental and Clinical Pharmacology. Unidade: FCFRP
Subjects: ÓXIDO NÍTRICO, AORTA DE ANIMAL, ENDOTÉLIO VASCULAR
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ABNT
KANGUSSU, Lucas M. et al. Enhancement on reactive oxygen species and COX-1 mRNA levels modulate the vascular relaxation induced by sodium nitroprusside in denuded mice aorta. Fundamental and Clinical Pharmacology, v. 29, n. 2, p. 150-163, 2015Tradução . . Disponível em: https://doi.org/10.1111/fcp.12103. Acesso em: 15 nov. 2024.
APA
Kangussu, L. M., Olivon, V. C., Arifa, R. D. do N., Araújo, N., Reis, D., Assis, M. T. de A., et al. (2015). Enhancement on reactive oxygen species and COX-1 mRNA levels modulate the vascular relaxation induced by sodium nitroprusside in denuded mice aorta. Fundamental and Clinical Pharmacology, 29( 2), 150-163. doi:10.1111/fcp.12103
NLM
Kangussu LM, Olivon VC, Arifa RD do N, Araújo N, Reis D, Assis MT de A, Soriani FM, Souza D da G de, Bendhack LM, Bonaventura D. Enhancement on reactive oxygen species and COX-1 mRNA levels modulate the vascular relaxation induced by sodium nitroprusside in denuded mice aorta [Internet]. Fundamental and Clinical Pharmacology. 2015 ; 29( 2): 150-163.[citado 2024 nov. 15 ] Available from: https://doi.org/10.1111/fcp.12103
Vancouver
Kangussu LM, Olivon VC, Arifa RD do N, Araújo N, Reis D, Assis MT de A, Soriani FM, Souza D da G de, Bendhack LM, Bonaventura D. Enhancement on reactive oxygen species and COX-1 mRNA levels modulate the vascular relaxation induced by sodium nitroprusside in denuded mice aorta [Internet]. Fundamental and Clinical Pharmacology. 2015 ; 29( 2): 150-163.[citado 2024 nov. 15 ] Available from: https://doi.org/10.1111/fcp.12103
Artigo de periodico
Pharmacological evidence of participation of nitric oxide in the vasorelaxant effect induced by D-arabinose oxime (2015)
Oliveira Júnior, Francisco Antônio; Pereira, Amanda Carvalho; Viana, Renato Márcio Ribeiro; Albuquerque, Katy Lisias Gondin Dias; Alves, Maria Angélica S. Gomes; Costa, Karla Veruska M. Cavalcante da; Gonçalves, Islania Gisélia Albuquerque; Alves, Ricardo José; Guedes, Diego Nunes; Bendhack, Lusiane Maria; Medeiros, Isac Almeida de; Correia, Nadja Azevêdo
Source: Journal of Pharmaceutical Biology. Unidade: FCFRP
Subjects: ÓXIDO NÍTRICO, VASODILATAÇÃO, ARTÉRIAS
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ABNT
OLIVEIRA JÚNIOR, Francisco Antônio et al. Pharmacological evidence of participation of nitric oxide in the vasorelaxant effect induced by D-arabinose oxime. Journal of Pharmaceutical Biology, v. 5, n. 1, p. 14-21, 2015Tradução . . Disponível em: http://www.jpbjournal.com/admin/fckeditor/_samples/php/article/159_14-21(jpb).pdf. Acesso em: 15 nov. 2024.
APA
Oliveira Júnior, F. A., Pereira, A. C., Viana, R. M. R., Albuquerque, K. L. G. D., Alves, M. A. S. G., Costa, K. V. M. C. da, et al. (2015). Pharmacological evidence of participation of nitric oxide in the vasorelaxant effect induced by D-arabinose oxime. Journal of Pharmaceutical Biology, 5( 1), 14-21. Recuperado de http://www.jpbjournal.com/admin/fckeditor/_samples/php/article/159_14-21(jpb).pdf
NLM
Oliveira Júnior FA, Pereira AC, Viana RMR, Albuquerque KLGD, Alves MASG, Costa KVMC da, Gonçalves IGA, Alves RJ, Guedes DN, Bendhack LM, Medeiros IA de, Correia NA. Pharmacological evidence of participation of nitric oxide in the vasorelaxant effect induced by D-arabinose oxime [Internet]. Journal of Pharmaceutical Biology. 2015 ; 5( 1): 14-21.[citado 2024 nov. 15 ] Available from: http://www.jpbjournal.com/admin/fckeditor/_samples/php/article/159_14-21(jpb).pdf
Vancouver
Oliveira Júnior FA, Pereira AC, Viana RMR, Albuquerque KLGD, Alves MASG, Costa KVMC da, Gonçalves IGA, Alves RJ, Guedes DN, Bendhack LM, Medeiros IA de, Correia NA. Pharmacological evidence of participation of nitric oxide in the vasorelaxant effect induced by D-arabinose oxime [Internet]. Journal of Pharmaceutical Biology. 2015 ; 5( 1): 14-21.[citado 2024 nov. 15 ] Available from: http://www.jpbjournal.com/admin/fckeditor/_samples/php/article/159_14-21(jpb).pdf
Artigo de periodico
Development of a method to quantify clindamycin in vitreous humor of rabbits' eyes by UPLC-MS/MS: application to a comparative pharmacokinetic study and in vivo ocular biocompatibility evaluation (2015)
Fernandes-Cunha, Gabriella M.; Gouvea, Dayana Rubio; Fulgêncio, Gustavo de Oliveira; Rezende, Cíntia M. F.; Silva, Gisele Rodrigues da; Bretas, Juliana M.; Fialho, Silvia Ligório; Lopes, Norberto Peporine; Silva-Cunha, Armando
Source: Journal of Pharmaceutical and Biomedical Analysis. Unidade: FCFRP
Subjects: CROMATOGRAFIA LÍQUIDA, ESPECTROMETRIA DE MASSAS, FARMACOCINÉTICA, TOXOPLASMOSE
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ABNT
FERNANDES-CUNHA, Gabriella M. et al. Development of a method to quantify clindamycin in vitreous humor of rabbits' eyes by UPLC-MS/MS: application to a comparative pharmacokinetic study and in vivo ocular biocompatibility evaluation. Journal of Pharmaceutical and Biomedical Analysis, v. 102, p. 346-352, 2015Tradução . . Disponível em: https://doi.org/10.1016/j.jpba.2014.08.023. Acesso em: 15 nov. 2024.
APA
Fernandes-Cunha, G. M., Gouvea, D. R., Fulgêncio, G. de O., Rezende, C. M. F., Silva, G. R. da, Bretas, J. M., et al. (2015). Development of a method to quantify clindamycin in vitreous humor of rabbits' eyes by UPLC-MS/MS: application to a comparative pharmacokinetic study and in vivo ocular biocompatibility evaluation. Journal of Pharmaceutical and Biomedical Analysis, 102, 346-352. doi:10.1016/j.jpba.2014.08.023
NLM
Fernandes-Cunha GM, Gouvea DR, Fulgêncio G de O, Rezende CMF, Silva GR da, Bretas JM, Fialho SL, Lopes NP, Silva-Cunha A. Development of a method to quantify clindamycin in vitreous humor of rabbits' eyes by UPLC-MS/MS: application to a comparative pharmacokinetic study and in vivo ocular biocompatibility evaluation [Internet]. Journal of Pharmaceutical and Biomedical Analysis. 2015 ; 102 346-352.[citado 2024 nov. 15 ] Available from: https://doi.org/10.1016/j.jpba.2014.08.023
Vancouver
Fernandes-Cunha GM, Gouvea DR, Fulgêncio G de O, Rezende CMF, Silva GR da, Bretas JM, Fialho SL, Lopes NP, Silva-Cunha A. Development of a method to quantify clindamycin in vitreous humor of rabbits' eyes by UPLC-MS/MS: application to a comparative pharmacokinetic study and in vivo ocular biocompatibility evaluation [Internet]. Journal of Pharmaceutical and Biomedical Analysis. 2015 ; 102 346-352.[citado 2024 nov. 15 ] Available from: https://doi.org/10.1016/j.jpba.2014.08.023
Artigo de periodico
The azo dye disperse red 13 and its oxidation and reduction products showed mutagenic potential (2015)
Chequer, Farah Maria Drumond; Lizier, Thiago Mescoloto; Felício, Rafael de; Zanoni, Maria Valnice Boldrin; Debonsi, Hosana Maria; Lopes, Norberto Peporine; Oliveira, Danielle Palma de
Source: Toxicology in Vitro. Unidade: FCFRP
Subjects: TOXICOLOGIA, CORANTES, MUTAGÊNESE, BIOTRANSFORMAÇÃO
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ABNT
CHEQUER, Farah Maria Drumond et al. The azo dye disperse red 13 and its oxidation and reduction products showed mutagenic potential. Toxicology in Vitro, v. 29, n. 7, p. 1906-1915, 2015Tradução . . Disponível em: https://doi.org/10.1016/j.tiv.2015.08.001. Acesso em: 15 nov. 2024.
APA
Chequer, F. M. D., Lizier, T. M., Felício, R. de, Zanoni, M. V. B., Debonsi, H. M., Lopes, N. P., & Oliveira, D. P. de. (2015). The azo dye disperse red 13 and its oxidation and reduction products showed mutagenic potential. Toxicology in Vitro, 29( 7), 1906-1915. doi:10.1016/j.tiv.2015.08.001
NLM
Chequer FMD, Lizier TM, Felício R de, Zanoni MVB, Debonsi HM, Lopes NP, Oliveira DP de. The azo dye disperse red 13 and its oxidation and reduction products showed mutagenic potential [Internet]. Toxicology in Vitro. 2015 ; 29( 7): 1906-1915.[citado 2024 nov. 15 ] Available from: https://doi.org/10.1016/j.tiv.2015.08.001
Vancouver
Chequer FMD, Lizier TM, Felício R de, Zanoni MVB, Debonsi HM, Lopes NP, Oliveira DP de. The azo dye disperse red 13 and its oxidation and reduction products showed mutagenic potential [Internet]. Toxicology in Vitro. 2015 ; 29( 7): 1906-1915.[citado 2024 nov. 15 ] Available from: https://doi.org/10.1016/j.tiv.2015.08.001
Artigo de periodico
Acute restraint stress increases carotid reactivity in type-I diabetic rats by enhancing Nox4/NADPH oxidase functionality (2015)
Moreira, Josimar D; Pernomian, Larissa; Gomes, Mayara Santos; Pernomian, Laena; Moreira, Rafael P; Prado, Alejandro F. do; Silva, Carlos Henrique Tomich de Paula da; Oliveira, Ana Maria de
Source: European Journal Pharmacology. Unidade: FCFRP
Subjects: SISTEMA RENINA-ANGIOTENSINA, ESTRESSE, DIABETES MELLITUS, ANGIOTENSINAS, DOENÇAS VASCULARES
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ABNT
MOREIRA, Josimar D et al. Acute restraint stress increases carotid reactivity in type-I diabetic rats by enhancing Nox4/NADPH oxidase functionality. European Journal Pharmacology, v. 765, p. 503-516, 2015Tradução . . Disponível em: https://doi.org/10.1016/j.ejphar.2015.09.020. Acesso em: 15 nov. 2024.
APA
Moreira, J. D., Pernomian, L., Gomes, M. S., Pernomian, L., Moreira, R. P., Prado, A. F. do, et al. (2015). Acute restraint stress increases carotid reactivity in type-I diabetic rats by enhancing Nox4/NADPH oxidase functionality. European Journal Pharmacology, 765, 503-516. doi:10.1016/j.ejphar.2015.09.020
NLM
Moreira JD, Pernomian L, Gomes MS, Pernomian L, Moreira RP, Prado AF do, Silva CHT de P da, Oliveira AM de. Acute restraint stress increases carotid reactivity in type-I diabetic rats by enhancing Nox4/NADPH oxidase functionality [Internet]. European Journal Pharmacology. 2015 ; 765 503-516.[citado 2024 nov. 15 ] Available from: https://doi.org/10.1016/j.ejphar.2015.09.020
Vancouver
Moreira JD, Pernomian L, Gomes MS, Pernomian L, Moreira RP, Prado AF do, Silva CHT de P da, Oliveira AM de. Acute restraint stress increases carotid reactivity in type-I diabetic rats by enhancing Nox4/NADPH oxidase functionality [Internet]. European Journal Pharmacology. 2015 ; 765 503-516.[citado 2024 nov. 15 ] Available from: https://doi.org/10.1016/j.ejphar.2015.09.020
Artigo de periodico
Rimonabant effects on anxiety induced by simulated public speaking in health humans: a preliminary report (2014)
Bergamaschi, Mateus M.; Queiroz, Regina Helena Costa; Chagas, Marcos Hortes Nisihara; Linares, Ila M. P.; Arrais, Kátia C.; Oliveira, Danielle C. G. de; Queiroz, Maria Eugênia Costa; Nardi, Antonio E.; Huestis, Marilyn A.; Hallak, Jaime Eduardo Cecílio; Zuardi, Antonio Waldo; Moreira, Fabrício A.; Crippa, José Alexandre de Souza
Source: Human Psychopharmacology. Unidades: FCFRP, FMRP, FFCLRP
Subjects: CANNABIS (COMPONENTES), ANTAGONISTAS, ANSIEDADE (TESTES)
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ABNT
BERGAMASCHI, Mateus M. et al. Rimonabant effects on anxiety induced by simulated public speaking in health humans: a preliminary report. Human Psychopharmacology, v. 29, n. 1, p. 94-99, 2014Tradução . . Disponível em: https://doi.org/10.1002/hup.2374. Acesso em: 15 nov. 2024.
APA
Bergamaschi, M. M., Queiroz, R. H. C., Chagas, M. H. N., Linares, I. M. P., Arrais, K. C., Oliveira, D. C. G. de, et al. (2014). Rimonabant effects on anxiety induced by simulated public speaking in health humans: a preliminary report. Human Psychopharmacology, 29( 1), 94-99. doi:10.1002/hup.2374
NLM
Bergamaschi MM, Queiroz RHC, Chagas MHN, Linares IMP, Arrais KC, Oliveira DCG de, Queiroz MEC, Nardi AE, Huestis MA, Hallak JEC, Zuardi AW, Moreira FA, Crippa JA de S. Rimonabant effects on anxiety induced by simulated public speaking in health humans: a preliminary report [Internet]. Human Psychopharmacology. 2014 ; 29( 1): 94-99.[citado 2024 nov. 15 ] Available from: https://doi.org/10.1002/hup.2374
Vancouver
Bergamaschi MM, Queiroz RHC, Chagas MHN, Linares IMP, Arrais KC, Oliveira DCG de, Queiroz MEC, Nardi AE, Huestis MA, Hallak JEC, Zuardi AW, Moreira FA, Crippa JA de S. Rimonabant effects on anxiety induced by simulated public speaking in health humans: a preliminary report [Internet]. Human Psychopharmacology. 2014 ; 29( 1): 94-99.[citado 2024 nov. 15 ] Available from: https://doi.org/10.1002/hup.2374
Artigo de periodico
Dipyrone metabolite 4-MAA induces hypothermia and inhibits PG'E IND.2'-dependent and -independent fever while 4-AA only blocks PG'E IND.2'-dependent fever (2014)
Malvar, David do C.; Aguiar, Fernando A.; Vaz, Artur de L. L.; Assis, Débora C. R.; Melo, Miriam Cristina Contin de; Jabor, Valquíria A. P.; Kalapothakis, Evanguedes; Ferreira, Sérgio Henrique; Clososki, Giuliano Cesar; Souza, Glória Emília Petto de
Source: British Journal of Pharmacology. Unidade: FCFRP
Subjects: HIPOTERMIA, HIPOTÁLAMO, FARMACOLOGIA
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ABNT
MALVAR, David do C. et al. Dipyrone metabolite 4-MAA induces hypothermia and inhibits PG'E IND.2'-dependent and -independent fever while 4-AA only blocks PG'E IND.2'-dependent fever. British Journal of Pharmacology, v. 171, n. 15, p. 3666-3679, 2014Tradução . . Disponível em: https://doi.org/10.1111/bph.12717. Acesso em: 15 nov. 2024.
APA
Malvar, D. do C., Aguiar, F. A., Vaz, A. de L. L., Assis, D. C. R., Melo, M. C. C. de, Jabor, V. A. P., et al. (2014). Dipyrone metabolite 4-MAA induces hypothermia and inhibits PG'E IND.2'-dependent and -independent fever while 4-AA only blocks PG'E IND.2'-dependent fever. British Journal of Pharmacology, 171( 15), 3666-3679. doi:10.1111/bph.12717
NLM
Malvar D do C, Aguiar FA, Vaz A de LL, Assis DCR, Melo MCC de, Jabor VAP, Kalapothakis E, Ferreira SH, Clososki GC, Souza GEP de. Dipyrone metabolite 4-MAA induces hypothermia and inhibits PG'E IND.2'-dependent and -independent fever while 4-AA only blocks PG'E IND.2'-dependent fever [Internet]. British Journal of Pharmacology. 2014 ; 171( 15): 3666-3679.[citado 2024 nov. 15 ] Available from: https://doi.org/10.1111/bph.12717
Vancouver
Malvar D do C, Aguiar FA, Vaz A de LL, Assis DCR, Melo MCC de, Jabor VAP, Kalapothakis E, Ferreira SH, Clososki GC, Souza GEP de. Dipyrone metabolite 4-MAA induces hypothermia and inhibits PG'E IND.2'-dependent and -independent fever while 4-AA only blocks PG'E IND.2'-dependent fever [Internet]. British Journal of Pharmacology. 2014 ; 171( 15): 3666-3679.[citado 2024 nov. 15 ] Available from: https://doi.org/10.1111/bph.12717
Artigo de periodico
Arsenic removal from contaminated water by ultrafine δ-FeOOH adsorbents (2014)
Faria, Márcia Cristina da Silva; Rosemberg , Renedy S.; Bomfeti, Cleide A.; Monteiro, Douglas Santos; Barbosa Júnior, Fernando; Oliveira, Luiz Carlos Alves de; Rodriguez, Mariandry; Pereira, Márcio C.; Rodrigues, Jairo Lisboa
Source: Chemical Engineering Journal. Unidade: FCFRP
Subjects: ADSORÇÃO (TRATAMENTO DE ÁGUA), NANOPARTÍCULAS, TOXICOLOGIA AMBIENTAL
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ABNT
FARIA, Márcia Cristina da Silva et al. Arsenic removal from contaminated water by ultrafine δ-FeOOH adsorbents. Chemical Engineering Journal, v. 237, p. 47\201354, 2014Tradução . . Disponível em: https://doi.org/10.1016/j.cej.2013.10.006. Acesso em: 15 nov. 2024.
APA
Faria, M. C. da S., Rosemberg , R. S., Bomfeti, C. A., Monteiro, D. S., Barbosa Júnior, F., Oliveira, L. C. A. de, et al. (2014). Arsenic removal from contaminated water by ultrafine δ-FeOOH adsorbents. Chemical Engineering Journal, 237, 47\201354. doi:10.1016/j.cej.2013.10.006
NLM
Faria MC da S, Rosemberg RS, Bomfeti CA, Monteiro DS, Barbosa Júnior F, Oliveira LCA de, Rodriguez M, Pereira MC, Rodrigues JL. Arsenic removal from contaminated water by ultrafine δ-FeOOH adsorbents [Internet]. Chemical Engineering Journal. 2014 ; 237 47\201354.[citado 2024 nov. 15 ] Available from: https://doi.org/10.1016/j.cej.2013.10.006
Vancouver
Faria MC da S, Rosemberg RS, Bomfeti CA, Monteiro DS, Barbosa Júnior F, Oliveira LCA de, Rodriguez M, Pereira MC, Rodrigues JL. Arsenic removal from contaminated water by ultrafine δ-FeOOH adsorbents [Internet]. Chemical Engineering Journal. 2014 ; 237 47\201354.[citado 2024 nov. 15 ] Available from: https://doi.org/10.1016/j.cej.2013.10.006
Artigo de periodico
Combined immunization using DNA-Sm 14 and DNA-Hsp65 increases CD8+ memory T cells reduces chronic pathology and decreases egg viability during Schistosoma mansoni infection (2014)
Espíndola, Milena Sobral; Frantz, Fabiani Gai; Soares, Luana Silva; Masson, Ana Paula; Tefé-Silva, Cristiane; Bitencourt, Claudia Silva; Oliveira, Sérgio Costa; Rodrigues, Vanderlei; Ramos, Simone Gusmão; Silva, Célio Lopes; Faccioli, Lucia Helena
Source: BMC Infectious Diseases. Unidades: FCFRP, FMRP
Subjects: SCHISTOSOMA MANSONI, VACINAÇÃO (MÉTODOS), PROTEÍNAS DE TRANSPORTE, LINFÓCITOS T
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ABNT
ESPÍNDOLA, Milena Sobral et al. Combined immunization using DNA-Sm 14 and DNA-Hsp65 increases CD8+ memory T cells reduces chronic pathology and decreases egg viability during Schistosoma mansoni infection. BMC Infectious Diseases, v. 14, 2014Tradução . . Disponível em: https://doi.org/10.1186/1471-2334-14-263. Acesso em: 15 nov. 2024.
APA
Espíndola, M. S., Frantz, F. G., Soares, L. S., Masson, A. P., Tefé-Silva, C., Bitencourt, C. S., et al. (2014). Combined immunization using DNA-Sm 14 and DNA-Hsp65 increases CD8+ memory T cells reduces chronic pathology and decreases egg viability during Schistosoma mansoni infection. BMC Infectious Diseases, 14. doi:10.1186/1471-2334-14-263
NLM
Espíndola MS, Frantz FG, Soares LS, Masson AP, Tefé-Silva C, Bitencourt CS, Oliveira SC, Rodrigues V, Ramos SG, Silva CL, Faccioli LH. Combined immunization using DNA-Sm 14 and DNA-Hsp65 increases CD8+ memory T cells reduces chronic pathology and decreases egg viability during Schistosoma mansoni infection [Internet]. BMC Infectious Diseases. 2014 ; 14[citado 2024 nov. 15 ] Available from: https://doi.org/10.1186/1471-2334-14-263
Vancouver
Espíndola MS, Frantz FG, Soares LS, Masson AP, Tefé-Silva C, Bitencourt CS, Oliveira SC, Rodrigues V, Ramos SG, Silva CL, Faccioli LH. Combined immunization using DNA-Sm 14 and DNA-Hsp65 increases CD8+ memory T cells reduces chronic pathology and decreases egg viability during Schistosoma mansoni infection [Internet]. BMC Infectious Diseases. 2014 ; 14[citado 2024 nov. 15 ] Available from: https://doi.org/10.1186/1471-2334-14-263
Artigo de periodico
Complexes of platinum and palladium with 'beta'-diketones and DMSO: synthesis, characterization, molecular modeling, and biological studies (2014)
Almeida, J. do Couto; Marzano, I. M.; Silva de Paula, F. C.; Pivatto, M.; Lopes, Norberto Peporine; Souza, P. C. de; Pavan, F. R.; Formiga, A. L. B.; Pereira-Maia, E. C.; Guerra, W.
Source: Journal of Molecular Structure. Unidade: FCFRP
Subjects: MODELAGEM MOLECULAR, MICOBACTERIOSE, CITOTOXINAS (ATIVIDADE)
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ABNT
ALMEIDA, J. do Couto et al. Complexes of platinum and palladium with 'beta'-diketones and DMSO: synthesis, characterization, molecular modeling, and biological studies. Journal of Molecular Structure, v. 1075, p. 370-376, 2014Tradução . . Disponível em: https://doi.org/10.1016/j.molstruc.2014.07.023. Acesso em: 15 nov. 2024.
APA
Almeida, J. do C., Marzano, I. M., Silva de Paula, F. C., Pivatto, M., Lopes, N. P., Souza, P. C. de, et al. (2014). Complexes of platinum and palladium with 'beta'-diketones and DMSO: synthesis, characterization, molecular modeling, and biological studies. Journal of Molecular Structure, 1075, 370-376. doi:10.1016/j.molstruc.2014.07.023
NLM
Almeida J do C, Marzano IM, Silva de Paula FC, Pivatto M, Lopes NP, Souza PC de, Pavan FR, Formiga ALB, Pereira-Maia EC, Guerra W. Complexes of platinum and palladium with 'beta'-diketones and DMSO: synthesis, characterization, molecular modeling, and biological studies [Internet]. Journal of Molecular Structure. 2014 ; 1075 370-376.[citado 2024 nov. 15 ] Available from: https://doi.org/10.1016/j.molstruc.2014.07.023
Vancouver
Almeida J do C, Marzano IM, Silva de Paula FC, Pivatto M, Lopes NP, Souza PC de, Pavan FR, Formiga ALB, Pereira-Maia EC, Guerra W. Complexes of platinum and palladium with 'beta'-diketones and DMSO: synthesis, characterization, molecular modeling, and biological studies [Internet]. Journal of Molecular Structure. 2014 ; 1075 370-376.[citado 2024 nov. 15 ] Available from: https://doi.org/10.1016/j.molstruc.2014.07.023
Artigo de periodico
Design, synthesis and enzymatic evaluation of 3-O-substituted aryl β-d-galactopyranosides as inhibitors of Trypanosoma cruzi trans-sialidase (2014)
Silva, Bruno L; S. Filho, José D; Andrade, Peterson; Carvalho, Ivone; Alves , Ricardo J
Source: Bioorganic & Medicinal Chemistry Letters. Unidade: FCFRP
Subjects: INIBIDORES DE ENZIMAS (FARMACOLOGIA), GLICOPROTEÍNAS (ANTAGONISTAS E INIBIDORES), TRYPANOSOMA CRUZI (ENZIMOLOGIA)
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ABNT
SILVA, Bruno L et al. Design, synthesis and enzymatic evaluation of 3-O-substituted aryl β-d-galactopyranosides as inhibitors of Trypanosoma cruzi trans-sialidase. Bioorganic & Medicinal Chemistry Letters, v. 24, n. 18, p. 4529-4532, 2014Tradução . . Disponível em: https://doi.org/10.1016/j.bmcl.2014.07.088. Acesso em: 15 nov. 2024.
APA
Silva, B. L., S. Filho, J. D., Andrade, P., Carvalho, I., & Alves , R. J. (2014). Design, synthesis and enzymatic evaluation of 3-O-substituted aryl β-d-galactopyranosides as inhibitors of Trypanosoma cruzi trans-sialidase. Bioorganic & Medicinal Chemistry Letters, 24( 18), 4529-4532. doi:10.1016/j.bmcl.2014.07.088
NLM
Silva BL, S. Filho JD, Andrade P, Carvalho I, Alves RJ. Design, synthesis and enzymatic evaluation of 3-O-substituted aryl β-d-galactopyranosides as inhibitors of Trypanosoma cruzi trans-sialidase [Internet]. Bioorganic & Medicinal Chemistry Letters. 2014 ; 24( 18): 4529-4532.[citado 2024 nov. 15 ] Available from: https://doi.org/10.1016/j.bmcl.2014.07.088
Vancouver
Silva BL, S. Filho JD, Andrade P, Carvalho I, Alves RJ. Design, synthesis and enzymatic evaluation of 3-O-substituted aryl β-d-galactopyranosides as inhibitors of Trypanosoma cruzi trans-sialidase [Internet]. Bioorganic & Medicinal Chemistry Letters. 2014 ; 24( 18): 4529-4532.[citado 2024 nov. 15 ] Available from: https://doi.org/10.1016/j.bmcl.2014.07.088

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